Tumor repolarization by an advanced liposomal drug delivery system provides a potent new approach for chemo-immunotherapy

L. Ringgaard, F. Melander, R. Eliasen, J.R. Henriksen, R.I. Jølck, T.B. Engel, M. Bak, F. P. Fliedner, K. Kristensen, Dennis Ringkjøbing Elema, A. Kjaer, A.E. Hansen, T.L. Andresen*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Immunosuppressive cells in the tumor microenvironment allow cancer cells to escape immune recognition and support cancer progression and dissemination. To improve therapeutic efficacy, we designed a liposomal oxaliplatin formulation (PCL8-U75) that elicits cytotoxic effects toward both cancer and immunosuppressive cells via protease-mediated, intratumoral liposome activation. The PCL8-U75 liposomes displayed superior therapeutic efficacy across all syngeneic cancer models in comparison to free-drug and liposomal controls. The PCL8-U75 depleted myeloid-derived suppressor cells and tumor-associated macrophages in the tumor microenvironment. The combination of improved cancer cell cytotoxicity and depletion of immunosuppressive populations of immune cells is attractive for combination with immune-activating therapy. Combining the PCL8-U75 liposomes with a TLR7 agonist induced immunological rejection of established tumors. This combination therapy increased intratumoral numbers of cancer antigen-specific cytotoxic T cells and Foxp3-T helper cells. These results are encouraging toward advancing liposomal drug delivery systems with anticancer and immune-modulating properties into clinical cancer therapy.
Original languageEnglish
Article numbereaba5628
JournalScience Advances
Issue number36
Number of pages12
Publication statusPublished - 2020


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